Mercurial > repos > saskia-hiltemann > cgatools_v17
annotate tools/cgatools17/testvariants_v17.xml @ 15:b5c879e950f5 draft default tip
planemo upload for repository https://bitbucket.org/EMCbioinf/galaxy-tool-shed-tools commit 402ebee914f2286aa9d98223f501f06c1e4b9c22-dirty
author | yhoogstrate |
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date | Fri, 20 Nov 2015 03:50:36 -0500 |
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planemo upload for repository https://bitbucket.org/EMCbioinf/galaxy-tool-shed-tools commit 18aaf80ea6ec743f134895c4a9a098a9e6146710-dirty
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1 <tool id="cg_testvariants" name="TestVariants" version="1.7.1.b"> |
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2 <description>Test for the presence of variants</description> |
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4 <requirements> |
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5 <requirement type="package" version="1">cgatools17</requirement> |
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6 </requirements> |
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7 |
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8 <version_command>cgatools | head -1</version_command> |
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9 |
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10 <command> |
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11 cgatools testvariants |
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12 --beta |
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13 --reference |
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14 |
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15 #if $reference_gene_sets_source.source_select == "indexed_filtered" |
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16 ${reference_gene_sets_source.crr.fields.crr_path} |
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17 #else if $reference_gene_sets_source.source_select == "history" |
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18 ${reference_gene_sets_source.crr} |
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19 #end if |
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20 |
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21 --output $output |
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22 --input $listing |
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23 --variants |
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24 #for $v in $file_types.varfiles <!--get each var/mastervar file--> |
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25 ${v.input} |
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26 #end for |
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27 </command> |
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28 |
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29 <inputs> |
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30 <!--form field to select crr file--> |
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31 |
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32 <conditional name="reference_gene_sets_source"> |
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33 <param name="source_select" type="select" label="GFF/GTF Source"> |
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34 <option value="indexed_filtered">Use a built-in index (which fits your reference)</option> |
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35 <option value="history">Use reference from the history</option> |
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36 </param> |
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37 <when value="indexed_filtered"> |
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38 <param name="crr" type="select" label="Reference Build"> |
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39 <options from_data_table="cg_anno_files" /> |
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40 </param> |
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41 </when> |
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42 <when value="history"> |
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43 <param name="crr" format="crr" type="data" label="Reference build" help="In crr format (you can use fasta2crr for conversion)" /> |
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44 </when> |
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45 </conditional> |
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46 |
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47 <!--form fields to select variant list--> |
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48 <param name="listing" type="data" format="tabular" label="Select variant list"/> |
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49 |
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50 <!--conditional to select input file type--> |
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51 <conditional name="file_types"> |
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52 <param name="file_type" type="select" label="Select the input file type"> |
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53 <option value="var" selected="true">var files</option> |
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54 <option value="mastervar">mastervar files</option> |
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55 </param> |
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56 <when value="var"> |
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57 <repeat name="varfiles" title="Variant files"> |
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58 <param name="input" type="data" format="cg_var" label="Dataset"/> |
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59 </repeat> |
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60 </when> |
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61 <when value="mastervar"> |
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62 <repeat name="varfiles" title="Variant files"> |
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63 <param name="input" type="data" format="cg_mastervar" label="Dataset"/> |
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64 </repeat> |
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65 </when> |
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66 </conditional> |
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67 |
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68 <!-- prefix for output file so you dont have to manually rename history items --> |
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69 <param name="fname" type="text" value="" label="Prefix for your output file" help="Optional"/> |
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70 </inputs> |
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71 |
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72 |
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73 <outputs> |
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74 <data format="tabular" name="output" label="$fname ${tool.name} on ${on_string}"/> |
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75 </outputs> |
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76 |
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77 <help> |
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78 **What it does** |
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79 |
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80 This tool uses the cgatools testvariants to test variant or mastervar files for the presence of variants. |
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81 |
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82 **cgatools 1.7.1 Documentation** |
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83 |
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84 Userguide: http://cgatools.sourceforge.net/docs/1.7.1/cgatools-user-guide.pdf |
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85 |
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86 Release notes: http://cgatools.sourceforge.net/docs/1.7.1/cgatools-release-notes.pdf |
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87 |
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88 **Command line reference**:: |
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89 |
3
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90 COMMAND NAME |
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91 testvariants - Tests variant files for presence of variants. |
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92 |
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93 DESCRIPTION |
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94 Tests variant files for presence of variants. The output is a tab-delimited |
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95 file consisting of the columns of the input variants file, plus a column |
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96 for each assembly results file that contains a character code for each |
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97 allele. The character codes have meaning as follows: |
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98 |
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99 0 This allele of this genome is consistent with the reference at this |
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100 locus but inconsistent with the variant. |
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101 1 This allele of this genome has the input variant at this locus. |
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102 N This allele of this genome has no-calls but is consistent with the |
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103 input variant. |
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104 |
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105 OPTIONS |
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106 -h [ --help ] |
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107 Print this help message. |
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108 |
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109 --beta |
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110 This is a beta command. To run this command, you must pass the --beta |
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111 flag. |
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112 |
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113 --reference arg |
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114 The reference crr file. |
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115 |
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116 --input arg (=STDIN) |
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117 The input variants to test for. |
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118 |
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119 --output arg (=STDOUT) |
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120 The output file (may be omitted for stdout). |
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121 |
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122 --variants arg |
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123 The input variant files (may be passed in as arguments at the end of |
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124 the command). |
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125 |
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126 SUPPORTED FORMAT_VERSION |
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127 0.3 or later |
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128 </help> |
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129 </tool> |